WO2020024826A1 - Synergistic antitumor effect of bcl-2 inhibitor combined with rituximab and/or bendamustine or bcl-2 inhibitor combined with chop - Google Patents
Synergistic antitumor effect of bcl-2 inhibitor combined with rituximab and/or bendamustine or bcl-2 inhibitor combined with chop Download PDFInfo
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- WO2020024826A1 WO2020024826A1 PCT/CN2019/097028 CN2019097028W WO2020024826A1 WO 2020024826 A1 WO2020024826 A1 WO 2020024826A1 CN 2019097028 W CN2019097028 W CN 2019097028W WO 2020024826 A1 WO2020024826 A1 WO 2020024826A1
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- 0 C*c1c[n](*)c(*)c1 Chemical compound C*c1c[n](*)c(*)c1 0.000 description 17
- QIMMUPPBPVKWKM-UHFFFAOYSA-N Cc1cc(cccc2)c2cc1 Chemical compound Cc1cc(cccc2)c2cc1 QIMMUPPBPVKWKM-UHFFFAOYSA-N 0.000 description 2
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Definitions
- the invention belongs to the technical field of medical technology, and particularly relates to a combination product comprising a Bcl-2 inhibitor, an anti-CD20 antibody and/or bendamustine or a combination product comprising a Bcl-2 inhibitor and CHOP, the combination product provides for a use in the prevention and/or treatment of diseases (e.g, cancers, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis) .
- diseases e.g, cancers, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis
- Apoptosis (programmed cell death) is a natural pathway for the body to clear abnormal or unwanted cells, which can cause various diseases such as cancers if affected.
- Bcl-2 proteins are associated with many diseases.
- Bcl-2 family proteins are key regulators in the mitochondria-mediated apoptotic pathway. Escape from apoptosis is one of the characteristics of human cancers and is a common cause of clinical drug resistances.
- BCL-2 protein In approximately one-third of patients with diffuse large B-cell lymphoma (DLBCL) , BCL-2 protein is highly expressed. Therefore, targeting BCL-2 protein to induce apoptosis is considered to be an effective method for treating B cell lymphoid malignancies.
- long-term use of BCL-2 inhibitors may induce drug resistance.
- the mechanisms of drug resistance include induction of expression of other anti-apoptotic proteins, such as MCL-1 and BCL-XL, continuous activation of intracellular signaling (i.e, downstream BCR signaling) , etc. (Youle RJ, Strasser A. The BCL-2 protein family: opposing activities that mediate cell death. Nat Rev Mol Cell Biol. 2008; 9 (1) : 47-59) .
- the present invention provides a combination product comprising a Bcl-2 inhibitor, an anti-CD20 antibody and/or bendamustine, or a combination product comprising a Bcl-2 inhibitor and CHOP, the combination product provides for a use in the prevention and/or treatment of diseases (e.g, cancers, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis) .
- diseases e.g, cancers, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis
- a first aspect of the invention relates to a combination product comprising a Bcl-2 inhibitor and an anti-CD20 mAb. Also, the present invention relates to a combination product comprising a Bcl-2 inhibitor, an anti-CD20 mAb and bendamustine. Further, the present invention relates to a combination product comprising a Bcl-2 inhibitor and CHOP (cyclophosphamide, doxorubicin, vincristine and prednisone) .
- CHOP cyclophosphamide, doxorubicin, vincristine and prednisone
- the Bcl-2 inhibitor is a compound of Formula I-A or a pharmaceutically acceptable salt or solvate thereof:
- E is a carbon atom and is a double bond
- E is a -C (H) -and is a single bond
- E is a nitrogen atom and is a single bond
- R 1a and R 1b taken together with the carbon atom to which they are attached form a 3-, 4-, or 5-membered optionally substituted aliphatic ring; or
- R 1a and R 1b taken together with the carbon atom to which they are attached form a 4-or 5-membered optionally substituted heterocyclo;
- R 2 is selected from the group consisting of -NO 2 , -SO 2 CH 3 , and -SO 2 CF 3 ;
- R 2a is selected from the group consisting of hydrogen and X;
- R 3 is selected from the group consisting of hydrogen, -CN, -C ⁇ CH, and -N (R 4a ) (R 4b ) ;
- R 4a is selected from the group consisting of optionally substituted C 1-6 alkyl, optionally substituted C 3-6 cycloalkyl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl;
- R 4b is selected from the group consisting of hydrogen and C 1-4 alkyl
- R 5 is selected from the group consisting of is selected from the group consisting of optionally substituted C 1-6 alkyl, heterocyclo, cycloalkylalkyl, and heterocycloalkyl;
- R 6a , R 6c , R 6e , R 6f , and R 6g are each independently selected from the group consisting of hydrogen, optionally substituted C 1-6 alkyl, optionally substituted C 3-6 cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl;
- R 6b and R 6d are each independently selected from the group consisting of hydrogen, C 1-4 alkyl, and halogen;
- R 7 is selected from the group consisting of optionally substituted C 1-6 alkyl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl;
- R 8 is selected from the group consisting of hydrogen and halogen.
- the Bcl-2 inhibitor is selected from the group consisting of the following compounds or pharmaceutically acceptable salts or solvates thereof:
- the Bcl-2 inhibitor is the following compound or a pharmaceutically acceptable salt or solvate thereof:
- the anti-CD20 mAb is selected from the group consisting of: Rituximab, IF5, Ibritumomab tiuxetan, tositumomab, ocrelizumab, veltuzumab, ofatumumab, obinutuzumab, AME133V, Pro13192 and GA101, TRU-015.
- the combination product is in the form of a pharmaceutical composition.
- the Bcl-2 inhibitor and the anti-CD20 mAb are each in a separate preparation.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine are each in a separate preparation.
- the Bcl-2 inhibitor and CHOP are each in a separate preparation.
- the Bcl-2 inhibitor and anti-CD20 mAb are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor and CHOP are administered simultaneously, sequentially or alternately.
- the combination product further comprises a pharmaceutically acceptable carrier, diluent or excipient.
- the combined product is in the form of tablet, capsule, granule, syrup, powder, lozenge, sachet, cachet, elixir, suspension, emulsion, solution, syrup, aerosol, ointment, cream and injection.
- a second aspect of the invention relates to the use of a Bcl-2 inhibitor and an anti-CD20 mAb in the manufacture of a medicament for the prevention and/or treatment of a disease selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- a disease selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the present invention relates to a use of a Bcl-2 inhibitor, an anti-CD20 mAb and bendamustine in the manufacture of a medicament for the prevention and/or treatment of a disease selected from the group consisting of cancer, rheumatoid arthritis (RA) ) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- a disease selected from the group consisting of cancer, rheumatoid arthritis (RA) ) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the present invention relates to the use of a Bcl-2 inhibitor and CHOP in the manufacture of a medicament for the prevention and/or treatment of a disease, wherein the disease is cancer.
- a third aspect of the invention relates to a combination product for the prevention and/or treatment of a disease, in which the combination product comprises a Bcl-2 inhibitor and an anti-CD20 mAb, and the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the combination product comprises a Bcl-2 inhibitor and an anti-CD20 mAb
- the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the present invention relates to a combination product for preventing and/or treatment of a disease, in which the combination product comprises a Bcl-2 inhibitor, an anti-CD20 mAb and Bendamustine, and the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the combination product comprises a Bcl-2 inhibitor, an anti-CD20 mAb and Bendamustine
- the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the present invention relates to a combination product for the prevention and/or treatment of a disease, in which the combination product comprises a Bcl-2 inhibitor and CHOP, and the disease is cancer.
- a fourth aspect of the invention relates to a method for the prevention and/or treatment of a disease comprising administering to a subject in need thereof a prophylactically and/or therapeutically effective amount of a Bcl-2 inhibitor and an anti-CD20 mAb, in which the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- RA rheumatoid arthritis
- GPA granulomatosis with polyangiitis
- microscopic polyangiitis microscopic polyangiitis
- the invention relates to a method for the prevention and/or treatment of a disease, comprising administering to a subject in need thereof a prophylactically and/or therapeutically effective amount of a Bcl-2 inhibitor, an anti-CD20 mAb and Bendamustine, in which the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- RA rheumatoid arthritis
- GPA granulomatosis with polyangiitis
- microscopic polyangiitis microscopic polyangiitis
- the present invention relates to a method for the prevention and/or treatment of a disease, comprising administering to a subject in need thereof a prophylactically and/or therapeutically effective amount of a Bcl-2 inhibitor and CHOP, and the disease is cancer.
- Figure 1 shows the anti-tumor effect (A) and body weight change (B) caused by Compound 6 alone or in combination with rituximab in a human Toledo (DLBCL) mouse xenograft model.
- Figure 2 shows the anti-tumor effect (A) and body weight change (B) caused by Compound 6 alone or in combination with rituximab in a human OCI-LY8 (DLBCL) mouse xenograft model.
- Figure 3 shows the anti-tumor effect (A) and body weight change (B) caused by Compound 6 alone or in combination with BR (bendamustine +rituximab) in a human OCI-LY8 (DLBCL) mouse xenograft model (B of BR means bendamustine, and R of BR is rituximab) .
- Figure 4 shows the anti-tumor effect (A) and body weight change (B) caused by Compound 6 alone or in combination with BR in a human DOHH2 (FL) mouse xenograft model.
- Figure 5 shows the anti-tumor effect (A) and body weight change (B) caused by Compound 6 alone or in combination with CHOP in a human DOHH2 (FL) mouse xenograft model.
- anti-CD mAb refers to an immunoglobulin, such as a monoclonal or polyclonal antibody from an animal or human specific to a CD20 receptor, a cell surface antigen or a cell surface determinant.
- pharmaceutically acceptable salt refers to a salt of a free acid or a free base, usually prepared by reacting the free base with a suitable organic or inorganic acid or by reacting the acid with a suitable organic or inorganic base. This term can be used in any of the compounds of the invention.
- Representative salts include: acetate, besylate, benzoate, bicarbonate, hydrogen sulfate, hydrogen tartrate, borate, bromide, calcium edetate, camphorsulfonate, carbonate, chloride, clavulanate, citrate, dihydrochloride, edetate, ethanedisulfonate, estolate, esylate, fumarate, glucoheptonate, gluconate, glutamate, glycol lylarsanilate, hexylresorcinate, hydrabamine, hydrobromide, hydrochloride, hydroxynaphthoate, iodide, isethionate, lactate, lactobionate, laurate, malate, maleate, mandelate, methanesulfonate, methylbromide, methylnitrate, methylsulfate, monopotassium maleate, mucate, naphthalenesulfonate,
- an acidic substituent such as -COOH, an ammonium salt, morpholine salt, sodium salt, potassium salt, barium salt, calcium salt or the like can be formed for use in a dosage form.
- a basic group for example, in a limonoid compound or a 1, 1-dimethylbiguanide
- an acidic salt can be formed, such as hydrochloride, hydrobromide, phosphate, sulfate, trifluoroacetate, trichloroacetate, acetate, oxalate, maleate, pyruvate, malonate, succinate, citrate, tartrate, fumarate, mandelate, benzoate, cinnamate, methanesulfonate, ethanesulfonate, picrate, and the like.
- prevention/preventing refers to a compound or medicament (e.g, a combination product as claimed herein) can reduce a frequency of a symptom of a medical condition in a subject or delay the onset thereof when it is applied to a disease or condition (e.g., cancer) , in comparison with a subject to which the compound or medicament is not applied.
- a disease or condition e.g., cancer
- treatment/treating refers to reducing, alleviating or ameliorating a symptoms of a disease or condition, ameliorating a symptom caused by a potential metabolism, inhibiting a disease or symptom, such as preventing a disease or a disorder from progression, ameliorating a disease or condition, causing regression of a disease or condition, alleviating a condition caused by a disease or condition, or preventing a symptom of a disease or condition.
- cancer refers to a neoplasm or tumor caused by abnormal, uncontrolled cell growth. Non-limiting examples include those exemplary cancers described in the detailed description of the invention.
- cancer includes diseases involving both pre-malignant cancer cells and malignant cancer cells.
- solvate is a combination, physical binding, and/or solvation of a compound of the invention with a solvent molecule, such as a disolvate, a monosolvate, a hemisolvate.
- a solvent molecule such as a disolvate, a monosolvate, a hemisolvate.
- the compounds of the present invention may be in a solvate form with a pharmaceutically acceptable solvent such as water, methanol, ethanol, etc., which does not significantly affect the pharmacological activity or toxicity of the compounds and which may act as a pharmacological equivalent.
- subject refers to including humans (e.g, patients) and animals (e.g, mice, rats, dogs, cats, rabbits, chickens, monkeys, etc. ) .
- Those of ordinary skill in the art can reasonably adjust the dose based on common sense and according to the specific weight of subject, the type and severity of disease, and other factors, and all of these adjusted technical solutions fall within the scope of the technical solutions claimed in the present invention.
- an "effective amount” or “prophylactically and/or therapeutically effective amount” as used herein refers to a sufficient amount (e.g, a dose) of a medicament or compound to be administered that will alleviate one or more symptoms of a disease or condition to be treated to some extent. The result can be a reduction and/or alleviation in the cause of the condition or disease or any other desired changes in biological system.
- an "effective amount” for therapeutic use is an amount of a compound or medicament (e.g, a combination product as claimed herein) that provides a significant reduction in the clinical symptoms of the disease or condition without causing excessive toxic side effects.
- dose refers to a weight (e.g, milligrams (mg) ) of an active substance per kilogram (kg) of a subject's body weight.
- IC 50 refers to an amount, concentration or dose of a particularly tested compound or medicament that achieves a 50%inhibition of maximum effect in an assay that measures such effect, for example inhibition of BCL-2 or BTK.
- room temperature refers to 25°C ⁇ 1°C. At the same time, if the experimental temperature is not specified, it is room temperature.
- aliphatic ring , "heterocycle” , “heterocycloalkyl” , “heteroalkyl” , “cycloalkylalkyl” and “halogen” as used herein have the ordinary meanings in the art, and a person of ordinary skill in the art will be able to understand the meaning thereof by the general knowledge or by reference to the prior art (for example, WO 2018/027097, the entire disclosure of which is incorporated herein by reference) .
- a first aspect of the invention relates to a combination product comprising or consisting of a Bcl-2 inhibitor and an anti-CD20 mAb.
- the present invention relates to a combination product comprising or consisting of a Bcl-2 inhibitor, an anti-CD20 mAb and bendamustine.
- the present invention relates to a combination product comprising or consisting of a Bcl-2 inhibitor and CHOP (cyclophosphamide, doxorubicin, vincristine and prednisone) .
- the Bcl-2 inhibitor is a compound of Formula I-A, or a pharmaceutically acceptable salt or solvate thereof:
- E is a carbon atom and is a double bond
- E is a -C (H) -and is a single bond
- E is a nitrogen atom and is a single bond
- R 1a and R 1b taken together with the carbon atom to which they are attached form a 3-, 4-, or 5-membered optionally substituted aliphatic ring; or
- R 1a and R 1b taken together with the carbon atom to which they are attached form a 4-or 5-membered optionally substituted heterocyclo;
- R 2 is selected from the group consisting of -NO 2 , -SO 2 CH 3 , and -SO 2 CF 3 ;
- R 2a is selected from the group consisting of hydrogen and X;
- R 3 is selected from the group consisting of hydrogen, -CN, -C ⁇ CH, and -N (R 4a ) (R 4b ) ;
- R 4a is selected from the group consisting of optionally substituted C 1-6 alkyl, optionally substituted C 3-6 cycloalkyl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl;
- R 4b is selected from the group consisting of hydrogen and C 1-4 alkyl
- R 5 is selected from the group consisting of is selected from the group consisting of optionally substituted C 1-6 alkyl, heterocyclo, cycloalkylalkyl, and heterocycloalkyl;
- R 6a , R 6c , R 6e , R 6f , and R 6g are each independently selected from the group consisting of hydrogen, optionally substituted C 1-6 alkyl, optionally substituted C 3-6 cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl;
- R 6b and R 6d are each independently selected from the group consisting of hydrogen, C 1-4 alkyl, and halogen;
- R 7 is selected from the group consisting of optionally substituted C 1-6 alkyl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl;
- R 8 is selected from the group consisting of hydrogen and halogen.
- X in the definition of variant R 2a refers to halogen.
- halogen mentioned above refers to F, Cl, Br, or I.
- the Bcl-2 inhibitor is a compound of Formula I-A, wherein: A is selected from the group consisting of A-1, A-2, A-3, A-4, A-5, A-6, A-7, A-8, and A-9; R 4a is selected from the group consisting of optionally substituted C 1-6 alkyl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl; and R 6a , R 6c , R 6e , R 6f and R 6g are each independently selected from the group consisting of hydrogen, optionally substituted C 1-6 alkyl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl.
- the Bcl-2 inhibitor is a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof,
- E is a carbon atom and is a double bond; or E is -C (H) -and is a single bond; or E is a nitrogen atom and is a single bond;
- R 1a and R 1b together with the carbon atom connected thereto form a 3-, 4-, or 5-membered optionally substituted aliphatic ring; or
- R 1a and R 1b together with the carbon atom connected thereto form a 4-or 5-membered optionally substituted heterocyclo
- R 2 is selected from the group consisting of -NO 2 , -SO 2 CH 3 , and -SO 2 CF 3 ;
- R 3 is selected from the group consisting of hydrogen, -CN, -C ⁇ CH, and -N (R 4a ) (R 4b ) ;
- R 4a is selected from the group consisting of optionally substituted C 1-6 alkyl, heterocyclo, cycloalkylalkyl, and heterocycloalkyl;
- R 4b is selected from the group consisting of hydrogen and C 1-4 alkyl.
- the Bcl-2 inhibitor is a compound of Formula II, or a pharmaceutically acceptable salt or solvate thereof,
- Y is selected from the group consisting of -CH 2 -and -O-, and R 2 and R 4a are as defined in connection with Formula I.
- the Bcl-2 inhibitor is a compound of Formula III, or a pharmaceutically acceptable salt or solvate thereof,
- Y is selected from the group consisting of -CH 2 -and -O-, and R 2 and R 4a are as defined in connection with Formula I.
- the Bcl-2 inhibitor is a compound of Formula IV, or a pharmaceutically acceptable salt or solvate thereof,
- Y is selected from the group consisting of -CH 2 -and -O-, and R 2 and R 4a are as defined in connection with Formula I.
- the Bcl-2 inhibitor is a compound of Formula V, or a pharmaceutically acceptable salt or solvate thereof,
- Y selected from the group consisting of -CH 2 -and -O-, and A, X 1 , X 2 , and X 3 are as defined in connection with Formula I-A.
- the Bcl-2 inhibitor is a compound of Formula VI, or a pharmaceutically acceptable salt or solvate thereof,
- Y selected from the group consisting of -CH 2 -and -O-, and A is as defined in connection with Formula I-A.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-1.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-2.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-3.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-4.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-5.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-6.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-7.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-8.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-9.
- the Bcl-2 inhibitor is a compound of Formula I-A, V or VI, or a pharmaceutically acceptable salt or solvate thereof, wherein A is A-10.
- the Bcl-2 inhibitor is a compound of Formula VII, or a pharmaceutically acceptable salt or solvate thereof,
- Y selected from the group consisting of -CH 2 -and -O-, and X 1 , X 2 , X 3 , R 2 , and R 4a are as defined in connection with Formula I-A.
- the Bcl-2 inhibitor is a compound of any one of Formulae II-VII, or a pharmaceutically acceptable salt or solvate thereof, wherein Y is -O-.
- the Bcl-2 inhibitor is a compound of any one of Formulae II-VII, or a pharmaceutically acceptable salt or solvate thereof, wherein Y is -CH 2 -.
- the Bcl-2 inhibitor is a compound of any one of Formulae I-A or I-VII, or a pharmaceutically acceptable salt or solvate thereof, wherein R 2 is -NO 2 .
- the Bcl-2 inhibitor is a compound of any one of Formulae I-VI, or a pharmaceutically acceptable salt or solvate thereof, wherein R 4a is selected from the group consisting of:
- the Bcl-2 inhibitor is a compound of any one of Formulae I-A or V-VII, or a pharmaceutically acceptable salt or solvate thereof, wherein R 4a , R 5 , R 6a , and R 7 are each independently selected from the group consisting of:
- the Bcl-2 inhibitor is a compound of Formula VIII, or a pharmaceutically acceptable salt or solvate thereof, wherein R 2a is hydrogen or fluoro and R 4a is as defined in connection with Formula I-A.
- the Bcl-2 inhibitor is a compound of Formula VIII, or a pharmaceutically acceptable salt or solvate thereof, wherein R 4a is selected from the group consisting of:
- the Bcl-2 inhibitor is a compound selected from one or more of the compounds of Table 1, or a pharmaceutically acceptable salt or solvate thereof.
- the Bcl-2 inhibitor is a compound selected from one or more of the compounds of Table 1-A, or a pharmaceutically acceptable salt or solvate thereof.
- the Bcl-2 inhibitor is a compound selected from one or more of the compounds of Table 1-B, or a pharmaceutically acceptable salt or solvate thereof.
- the anti-CD20 mAb is selected from the group consisting of: Rituximab, IF5, Ibritumomab tiuxetan, tositumomab, ocrelizumab, veltuzumab, ofatumumab, obinutuzumab, AME133V, Pro13192 and GA101, TRU-015; preferably, the anti-CD20 mAb is Rituximab.
- the combination product is in the form of a pharmaceutical composition.
- the Bcl-2 inhibitor and the anti-CD20 mAb are each in a separate preparation.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine are each in a separate preparation.
- the Bcl-2 inhibitor and CHOP are each in a separate preparation.
- the Bcl-2 inhibitor and anti-CD20 mAb are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor and CHOP are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor and anti-CD20 mAb may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 weeks, about 6 weeks, about 8 weeks, or about 12 weeks.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 weeks, about 6 weeks, about 8 weeks, or about 12 weeks.
- the Bcl-2 inhibitor and CHOP may be administered sequentially for about a time interval of 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 week, about 6 weeks, about 8 weeks, or about 12 weeks.
- the combination product of the invention comprising the Bcl-2 inhibitor and anti-CD20 mAb in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, can be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the combination product of the invention comprising the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, can be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the combination product of the invention comprising the Bcl-2 inhibitor and CHOP in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, can be daily administered for, including but not limited to, 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the combination product of the invention comprising the Bcl-2 inhibitor and anti-CD20 mAb in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, can be daily administered for, including but not limited to, 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the combination product of the invention comprising the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, can be daily administered for, including but not limited to, 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the combination product of the invention comprising the Bcl-2 inhibitor and CHOP in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, can be daily administered for, including but not limited to, 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the combination product can be administered in the following manner: oral, buccal, inhalation spray, sublingual, rectal, transdermal, vaginal mucosa, transmucosal, local, nasal or enteral administration; parenteral administration, such as intramuscular injection, subcutaneous injection, intramedullary injection, as well as intrathecal or brain direct administration, in situ administration, subcutaneous, intraperitoneal, intravenous injection, intra-articular synovium, intrasternal, intrahepatic, intralesional, intracranial, intra-abdominal, nasal, or intraocular injection or other drug delivery manners.
- parenteral administration such as intramuscular injection, subcutaneous injection, intramedullary injection, as well as intrathecal or brain direct administration, in situ administration, subcutaneous, intraperitoneal, intravenous injection, intra-articular synovium, intrasternal, intrahepatic, intralesional, intracranial, intra-abdominal, nasal, or intraocular injection or other drug delivery manners.
- the amount of the Bcl-2 inhibitor is 1 mg, 5 mg, 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 70 mg, 80 mg, 90 mg, 100 mg, 150 mg, 200 mg, 250 mg, 300 mg, 350 mg, 400 mg, 450 mg, 460 mg, 470 mg, 480 mg, 487 mg, 490 mg, 500 mg, 550 mg, 600 mg, 650 mg, 700 mg, 731 mg, 750 mg, 800 mg, 850 mg, 900 mg, 950 mg, 1000 mg, and a range between the respective amounts, for example, 1 mg to 1000 mg, 30 mg to 900 mg, 30 mg to 800 mg, 30 mg to 900 mg, 30 mg to 800 mg, 30 mg to 700 mg, 30 mg to 600 mg, 30 mg to 500 mg, 30 mg to 490 mg, 30 mg to 487 mg, 60 mg to 1000 mg, 60 mg to 900 mg, 60 mg to 800 mg, 60 mg to 731 mg, 731 mg to 1000 mg, etc.
- the amount of the anti-CD20 mAb is 1 mg, 5 mg, 10 mg, 15 mg, 16 mg, 17 mg, 18 mg, 19 mg, 19.5 mg, 20mg, 25mg, 30mg, 35mg, 40mg, 41 mg, 42mg, 43mg, 44mg, 45mg, 46mg, 47mg, 48mg, 48.8mg, 49mg, 50mg, 60mg, 70mg, 80mg, 90mg, 100mg, 150mg, 200mg, 250mg, 300 mg, 350 mg, 400 mg, 450 mg, 500 mg, 600 mg, 650 mg, 700 mg, 800 mg, and a range between the respective amounts, for example, 1 mg to 800 mg, 10 mg to 800 mg, 15 mg to 5800 mg, 19.5 mg to 700 mg, 19.5 mg to 500mg, 19.5mg to 300mg, 19.5mg to 100mg, 19.5 mg to 90 mg, 19.5 mg to 80 mg, 19.5 mg to 70 mg, 1
- the amount of the bendamustine is 1 mg, 5 mg, 10 mg, 20 mg, 30 mg, 40mg, 50mg, 60mg, 70mg, 80mg, 90mg, 100mg, 110mg, 120mg, 121.95mg, 150mg, 160, 180, 200mg, 250mg, 300mg, 350mg, 400mg, 450mg, 500mg, 550mg, 600mg, 650mg, 700mg, 750 mg, 800 mg, 850 mg, 900 mg, 950 mg, 1000 mg, and a range between the respective amounts, for example, 1 mg to 1000 mg, 50 mg to 900 mg, 100 mg to 800 mg, 121.95 mg to 1000 mg, 121.95 mg to 900 mg, 121.95 mg to 800 mg, 121.95 mg to 700 mg, 121.95 mg to 600 mg, 121.95 mg to 500 mg, 121.95 mg to 400 mg, 121.95 mg to 300 mg, 121.95 mg,
- the CHOP comprises: cyclophosphamide in an amount of 10 mg, 50 mg, 97.5 mg, 100 mg, 150 mg, and a range between the respective amounts, for example, 10 to 150 mg, 50 to 100 mg, 97.5 mg to 150 mg, etc. ; doxorubicin in an amount of 1 mg, 5 mg, 9.75 mg, 10 mg, 15 mg, and a range between the respective amounts, for example, 1 mg to 15 mg, 5 mg to 10 mg, 9.75 mg to 15 mg, etc.
- vincristine in an amount of 0.1 mg, 0.2 mg, 0.3 mg, 0.49 mg, 0.6 mg, 0.8 mg, 1 mg, 1.5 mg, and a range between the respective amounts, for example, 0.1 mg to 1.5 mg, 0.1 mg to 0.6 mg, 0.49 mg to 1.5 mg, etc.
- prednisone in an amount of 0.5 mg, 1 mg, 1.5 mg, 2.44 mg, 5 mg, 10 mg, and a range between the respective amounts, For example, 0.5 mg to 10 mg, 0.5 mg to 5 mg, 2.44 mg to 10 mg, and the like.
- the combination product further comprises a pharmaceutically acceptable carrier, diluent or excipient.
- the combination product is in the form of tablet, capsule, granule, syrup, powder, lozenge, sachet, cachet, elixir, suspension, emulsion, solution, syrup, aerosol, ointment, cream and injection.
- a second aspect of the invention relates to the use of a Bcl-2 inhibitor and an anti-CD20 mAb in the manufacture of a medicament for the prevention and/or treatment of a disease selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- a disease selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the present invention relates to the use of a Bcl-2 inhibitor, an anti-CD20 mAb and bendamustine in the manufacture of a medicament for the prevention and/or treatment of a disease selected from the group consisting of cancer and rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- a disease selected from the group consisting of cancer and rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the present invention relates to the use of a Bcl-2 inhibitor and CHOP in the manufacture of a medicament for the prevention and/or treatment of a disease, in which the disease is a cancer.
- the Bcl-2 inhibitor is a compound (e.g, Compound I-A) , or a pharmaceutically acceptable salt or solvate thereof, as specifically described in the first aspect of the invention.
- the anti-CD20 mAb is selected from the group consisting of: Rituximab, IF5, Ibritumomab tiuxetan, tositumomab, ocrelizumab, veltuzumab, ofatumumab, obinutuzumab, AME133V, Pro13192 and GA101, TRU-015.
- the anti-CD20 mAb is Rituximab.
- the drug is in the form of a pharmaceutical composition.
- the Bcl-2 inhibitor and the anti-CD20 mAb are each in a separate preparation.
- the Bcl-2 inhibitor, anti-CD20 mAb, and bendamustine are each in a separate preparation.
- the Bcl-2 inhibitor and CHOP are each in a separate preparation.
- the Bcl-2 inhibitor and anti-CD20 mAb are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor, anti-CD20 mAb, and bendamustine are administered simultaneously, sequentially, or alternately.
- the Bcl-2 inhibitor and CHOP are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor and anti-CD20 mAb may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 weeks, about 6 weeks, about 8 weeks, or about 12 weeks.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 weeks, about 6 weeks, about 8 weeks, or about 12 weeks.
- the Bcl-2 inhibitor and CHOP may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 Week, about 6 weeks, about 8 weeks, or about 12 weeks.
- the medicament of the present invention comprising the Bcl-2 inhibitor and anti-CD20 mAb in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor and CHOP in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor and anti-CD20 mAb in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor and CHOP in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament can be administered in the following manner: oral, buccal, inhalation spray, sublingual, rectal, transdermal, vaginal mucosa, transmucosal, local, nasal or enteral administration; parenteral administration, such as intramuscular injection, subcutaneous injection, intramedullary injection, as well as intrathecal or brain direct administration, in situ administration, subcutaneous, intraperitoneal, intravenous injection, intra-articular synovium, intrasternal, intrahepatic, intralesional, intracranial, intra-abdominal, nasal, or intraocular injection or other drug delivery manners.
- parenteral administration such as intramuscular injection, subcutaneous injection, intramedullary injection, as well as intrathecal or brain direct administration, in situ administration, subcutaneous, intraperitoneal, intravenous injection, intra-articular synovium, intrasternal, intrahepatic, intralesional, intracranial, intra-abdominal, nasal, or intraocular injection or other drug delivery manners.
- the Bcl-2 inhibitor or a pharmaceutically acceptable salt or solvate thereof, the anti-CD20 monoclonal antibody or a pharmaceutically acceptable salt or solvate thereof, the bendamustine or a pharmaceutically acceptable salt or solvate thereof, the CHOP (cyclophosphamide, doxorubicin, vincristine and prednisone) or a pharmaceutically acceptable salt or solvate thereof are administered in doses as described in the first aspect of the invention in the above detailed description of the invention.
- the disease is cancer.
- the cancer described in the present invention includes, but is not limited to, a cancer selected from the group consisting of: adrenal cancer, lymphoid epithelioma, acinic cell carcinoma, lymphoma, acoustic neuroma, acute lymphocytic leukemia, acral lentiginous melanoma, acute myelogeous leukemia, acrospiroma, chronic lymphocytic leukemia, acute eosinophilic leukemia, liver cancer, acute erythroid leukemia, small cell lung cancer, acute lymphoblastic leukemia, non-small cell lung cancer, acute megakaryoblastic leukemia, MALT lymphoma, acute monocytic leukemia, malignant fibrous histiocytoma, acute promyelocytic leukemia, malignant peripheral schwannomas, adenocarcinoma, malignant triton tumor, adenoid cystic carcinoma, mantle cell lymphoma, adenoma
- the cancer is selected from the group consisting of: acute monocytic leukemia, acute myeloid leukemia, chronic myelogenous leukemia, chronic lymphocytic leukemia and mixed lineage leukemia, NUT midline cancer, multiple myeloma, small cell lung cancer, neuroblastoma, Burkitt's lymphoma, cervical cancer, esophageal cancer, ovarian cancer, colorectal cancer, prostate cancer and breast cancer.
- the cancer is a hematological malignancy.
- the hematological malignancy is selected from the group consisting of: acute myeloid leukemia (AML) , acute lymphoblastic leukemia (ALL) , diffuse large B-cell lymphoma (DLBCL) , follicular lymphoma (FL) , chronic lymphocytic leukemia (CLL) /small lymphocytic lymphoma (SLL) , marginal zone lymphoma (MZL) , chronic myelogenous leukemia (CML) , mantle cell lymphoma (MCL) , Waldenstrom's macroglobulinemia (WM) .
- AML acute myeloid leukemia
- ALL acute lymphoblastic leukemia
- DLBCL diffuse large B-cell lymphoma
- FL follicular lymphoma
- FL follicular lymphoma
- CLL chronic lymphocytic leukemia
- SLL small lymphocytic lymphoma
- MZL marginal zone lymph
- the cancer is selected from the group consisting of bladder cancer, breast cancer, cervical cancer, colon cancer (including colorectal cancer) , esophageal cancer, head and neck cancer, liver cancer, lung cancer (small cell and non-small cell) , melanoma, myeloma, neuroblastoma, ovarian cancer, pancreatic cancer, prostate cancer, kidney cancer, sarcoma (including osteosarcoma) , skin cancer (including squamous cell carcinoma) , gastric cancer, testicular cancer, thyroid cancer, uterine cancer, mesothelioma, cholangiocarcinoma, leiomyosarcoma, liposarcoma, melanoma, nasopharyngeal carcinoma, neuroendocrine carcinoma, ovarian cancer, renal cancer, salivary gland cancer, or metastatic tumor caused by spindle cell carcinoma, non-Hodgkin's lymphoma, Hodgkin's lymphoma, and hemat
- the disease is rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- RA rheumatoid arthritis
- GPA granulomatosis with polyangiitis
- microscopic polyangiitis microscopic polyangiitis.
- a third aspect of the invention relates to a combination product for the prevention and/or treatment of a disease, in which the combination product comprises a Bcl-2 inhibitor and an anti-CD20 mAb, and the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the cancer includes, but is not limited to, those cancers as described in the second aspect of the invention in the above detailed description of the invention.
- the present invention relates to a combination product for the prevention and/or treatment of a disease, in which the combination product comprises a Bcl-2 inhibitor, an anti-CD20 mAb and bendamustine, and the disease is selected from the group consisting of cancer, Rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the combination product comprises a Bcl-2 inhibitor, an anti-CD20 mAb and bendamustine
- the disease is selected from the group consisting of cancer, Rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the present invention relates to a combination product for the prevention and/or treatment of a disease, in which the combination product comprises a Bcl-2 inhibitor and CHOP, and the disease is cancer.
- the Bcl-2 inhibitor is a compound (e.g, Compound I-A) , or a pharmaceutically acceptable salt or solvate thereof, as specifically described in the first aspect of the invention.
- the anti-CD20 mAb is selected from the group consisting of: Rituximab, IF5, Ibritumomab tiuxetan, tositumomab, ocrelizumab, veltuzumab, ofatumumab, obinutuzumab, AME133V, Pro13192 and GA101, TRU-015.
- the anti-CD20 mAb is Rituximab.
- the combination product is in the form of a pharmaceutical composition.
- the Bcl-2 inhibitor and the anti-CD20 mAb are each in a separate preparation.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine are each in a separate preparation.
- the Bcl-2 inhibitor and CHOP are each in a separate preparation.
- the Bcl-2 inhibitor and anti-CD20 mAb are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor and CHOP are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor and anti-CD20 mAb may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 weeks, about 6 weeks, about 8 weeks, or about 12 weeks.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 weeks, about 6 weeks, about 8 weeks, or about 12 weeks.
- the Bcl-2 inhibitor and CHOP may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 Week, about 6 weeks, about 8 weeks, or about 12 weeks.
- the medicament of the present invention comprising the Bcl-2 inhibitor and anti-CD20 mAb in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor and CHOP in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor and anti-CD20 mAb in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor and CHOP in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the combination product can be administered in the following manner: oral, buccal, inhalation spray, sublingual, rectal, transdermal, vaginal mucosa, transmucosal, topical, nasal or enteral administration; parenteral administration, such as intramuscular injection, subcutaneous injection, intramedullary injection, as well as intrathecal or brain direct administration, in situ administration, subcutaneous, intraperitoneal, intravenous injection, intra-articular synovium, intrasternal, intrahepatic, intralesional, intracranial, intra-abdominal, nasal, or intraocular injection or other drug delivery manners.
- parenteral administration such as intramuscular injection, subcutaneous injection, intramedullary injection, as well as intrathecal or brain direct administration, in situ administration, subcutaneous, intraperitoneal, intravenous injection, intra-articular synovium, intrasternal, intrahepatic, intralesional, intracranial, intra-abdominal, nasal, or intraocular injection or other drug delivery manners.
- the Bcl-2 inhibitor, or a pharmaceutically acceptable salt or solvate thereof, the anti-CD20 monoclonal antibody or a pharmaceutically acceptable salt or solvate thereof, the bendamustine or a pharmaceutically acceptable salt or solvate thereof, the CHOP (cyclophosphamide, doxorubicin, vincristine and prednisone) or a pharmaceutically acceptable salt or solvate thereof are administered in doses as described in the first aspect of the invention in the above detailed description of the invention.
- a fourth aspect of the invention relates to a method of preventing and/or treating a disease comprising administering to a subject in need thereof a prophylactically and/or therapeutically effective amount of the Bcl-2 inhibitor and anti-CD20 mAb, in which the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- the cancer includes, but is not limited to, those cancers as described in the second aspect of the invention in the above detailed description of the invention.
- the invention relates to a method of preventing and/or treating a disease comprising administering to a subject in need thereof a prophylactically and/or therapeutically effective amount of the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine, in which the disease is selected from the group consisting of cancers, autoimmune diseases, and inflammatory diseases.
- the present invention relates to a method of preventing and/or treating a disease comprising administering to a subject in need thereof a prophylactically and/or therapeutically effective amount of the Bcl-2 inhibitor and CHOP, in which the disease is cancer.
- the Bcl-2 inhibitor is a compound (e.g, Compound I-A) or a pharmaceutically acceptable salt or solvate thereof, as specifically described in the first aspect of the invention.
- the anti-CD20 mAb is selected from the group consisting of: Rituximab, IF5, Ibritumomab tiuxetan, tositumomab, ocrelizumab, veltuzumab, ofatumumab, obinutuzumab, AME133V, Pro13192 and GA101, TRU-015.
- the anti-CD20 mAb are Rituximab.
- the Bcl-2 inhibitor and anti-CD20 mAb are in the form of a pharmaceutical composition.
- the Bcl-2 inhibitor and the anti-CD20 mAb are each in a separate preparation.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine are each in a separate preparation.
- the Bcl-2 inhibitor and CHOP are each in a separate preparation.
- the Bcl-2 inhibitor and anti-CD20 mAb are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor and CHOP are administered simultaneously, sequentially or alternately.
- the Bcl-2 inhibitor and anti-CD20 mAb may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 weeks, about 6 weeks, about 8 weeks, or about 12 weeks.
- the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes., about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 weeks, about 6 weeks, about 8 weeks, or about 12 weeks.
- the Bcl-2 inhibitor and CHOP may be administered sequentially at a time interval of about 1 minute, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 24 hours, about 48 hours, about 72 hours, about 96 hours, about 1 week, about 2 weeks, about 3 weeks, about 4 weeks, about 5 week, about 6 weeks, about 8 weeks, or about 12 weeks.
- the medicament of the present invention comprising the Bcl-2 inhibitor and anti-CD20 mAb in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor and CHOP in the form of a pharmaceutical composition (preferably, each in a separate dosage unit form) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor and anti-CD20 mAb in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor, anti-CD20 mAb and bendamustine in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the medicament of the present invention comprising the Bcl-2 inhibitor and CHOP in the form of a pharmaceutical composition (preferably, in the form of a dosage unit) , as desired, may be daily administered for, including but not limited to: 1 time, 2 times, 3 times, 4 times, 5 times or 6 times.
- the Bcl-2 inhibitor, anti-CD20 mAb and CHOP can be administered in the following manner: oral, buccal, inhalation spray, sublingual, rectal, transdermal, vaginal mucosa, transmucosal, local, nasal or enteral administration; parenteral administration, such as intramuscular injection, subcutaneous injection, intramedullary injection, as well as intrathecal or brain direct administration, in situ administration, subcutaneous, intraperitoneal, intravenous injection, intra-articular synovium, intrasternal, intrahepatic, intralesional, intracranial, intra-abdominal, nasal, or intraocular injection or other drug delivery manners.
- the Bcl-2 inhibitor is administered daily at a dose of 0.017 mg/kg, 0.083 mg/kg, 0.17 mg/kg, 0.33 mg/kg, 0.5 mg/kg, 0.67 mg/kg, 0.83 mg/kg, 1 mg/kg, 1.16mg/kg, 1.33mg/kg, 1.5mg/kg, 1.67mg/kg, 2.5mg/kg, 3.33mg/kg, 4.17mg/kg, 5mg/kg, 5.83mg/kg, 6.67mg/kg, 7.5mg/kg, 7.67mg/kg, 7.83mg/kg, 8mg/kg, 8.12mg/kg, 8.16mg/kg, 8.33mg/kg, 9.17mg/kg, 10mg/kg, 10.83 mg/kg, 11.66 mg/kg, 12.5 mg/kg, 13.33 mg/kg, 14.17 mg/kg, 15 mg/kg, 15.83 mg/kg, 16.67 mg/kg, and a range between the respective doses, for example
- the daily administration dose of the anti-CD20 mAb is 0.16 mg/kg, 0.25 mg/kg, 0.325 mg, 0.41 mg/kg, 0.66 mg/kg, 0.75 mg/kg, 0.81 mg, 1 mg/kg, 1.33 mg/kg, 1.66 mg/kg, 3.33 mg/kg, 5mg/kg, 6.66mg/kg, 8.33mg kg, and a range between the respective doses, for example, 0.16mg to 8.33mg/kg, 0.16mg to 0.81 mg/kg, 0.325mg to 8.33mg/kg, 0.81 mg to 8.33mg/kg, 0.325 mg to 8.33 mg/kg, etc.
- the daily administration dose of bendamustine is 0.16 mg/kg, 0.83 mg/kg, 1.33 mg/kg, 1.66 mg/kg, 2.03 mg, 3.33 mg/kg, 5 mg/kg, 6.66 mg/kg, 8.33 mg/kg, 16.6 mg/kg, and a range between the respective doses, for example, 0.16 mg to 16.6 mg/kg, 0.16 mg to 2.03 mg/kg, 2.03 mg to 16.6 mg/kg, 2.03 mg to 16.6 mg/kg, etc.
- the CHOP includes: cyclophosphamide at a daily dose of 0.16 mg/kg, 0.83 mg/kg, 1.625 mg/kg, 1.66 mg/kg, 2.5 mg/kg, and a range between the respective doses, for example, 0.16 to 2.5 mg/kg, 0.83 to 2.5 mg/kg, 1.66 mg to 2.5 mg/kg, etc. ; doxorubicin at a daily dose of 0.016 mg/kg, 0.083 mg/kg, 0.162 mg/kg, 0.166 mg/kg, 0.25 mg/kg, and a range between the respective doses, for example, 0.016 mg to 0.25 mg/kg, 0.083 mg to 0.25 mg/kg, 0.162 mg to 0.25mg/kg, etc.
- WO 2018/027097 is incorporated by reference herein, in its entirety and for all purposes.
- the tumor cells were inoculated subcutaneously in the right flank of immunodeficient mice with a 1 mL syringe (4 gauge needle) , 5-10 ⁇ 10 6 /0.2 mL/mouse (experimental animals were purchased from Beijing Vital River Laboratory Animal Technology Co., Ltd., SCXK (Beijing) 2016 -0006) . All animal experiments were strictly in accordance with the laboratory animal use and management practices of GenePharma Co., Ltd. and Ascentage Pharma Group Co., Ltd. The calculation of relevant parameters referred to the Chinese CFDA "Guidelines for Non-Clinical Research Techniques of Cytotoxic Antitumor Drugs" .
- the animal body weight and tumor size were measured twice weekly during the experiment. The conditions and death of the animals were observed every day. Routine monitoring included the effects of tumor growth and treatment on normal animal behaviors, including activity, feeding and drinking situations, weight gain or loss, eyes, coat and other abnormalities in the experimental animals. The deaths and clinical symptoms observed during the experiment were recorded in the raw data. The entire operations of administration, measurement of mouse body weight and tumor volume were performed in a clean bench. Plasma and tumor tissues were collected, weighed and photographed after the end of the last administration according to the experimental protocol. Plasma and tumor samples were snap frozen and stored at -80°C.
- Change of body weight % (measured body weight -body weight at the time of grouping) /body weight at the time of grouping ⁇ 100%.
- synergy factor ( (A/C) ⁇ (B /C) ) / (AB /C) ;
- A RTV value of the group administered with A only;
- B RTV value of the group administered with B only;
- C RTV value of the vehicle control group;
- AB RTV value of the group administered with A and B in combination (Clarke R. Issues in experimental design and endpoint analysis in the study of experimental cytotoxic agents in vivo in breast cancer and other models [J] .
- Example 3 Effects of Compound 6 in combination with Rituximab (anti-CD20 antibody) in mouse xenograft tumor model
- Compound 6 in combination with rituximab had no significant side effects (Figure 1 B) , but significantly increased the anti-tumor effect of single drug in human Toledo (DLBCL) mouse xenograft tumor model, with significant synergistic effect (synergistic factor was 1.37, greater than 1) . Therefore, the combination of Compound 6 with rituximab may clinically benefit patients with diffuse large B-cell lymphoma (DLBCL) .
- DLBCL diffuse large B-cell lymphoma
- OCI-LY8 showed a rapidly growing xenograft tumor, and on the 11th day after administration, the control animals were euthanized because the tumor volume exceeded the limit allowed by the animal welfare.
- Four out of five animals acheived PR was 80%) .
- T/C values of Compound 6 in combination with rituximab at doses of 50 mg/kg and 100 mg/kg were 3%(P ⁇ 0.001) and 2% (P ⁇ 0.001) , respectively.
- PR was observed in 6/6 of the animals (remission rate was 100%) .
- T/C RTV values of combination group at 50 mg/kg (Compound 6) or 100 mg/kg (Compound 6) were 23%(P ⁇ 0.05) and 15% (P ⁇ 0.05) , respectively, indicating a significant increase in the inhibition of tumor growth by the two combination groups.
- Compound 6 in combination with rituximab had no significant side effects (Figure 2B) and significantly increased the anti-tumor effect in comparison with the single arm of Compound 6 or rituximab in the OCI-LY8 human DLBCL cell mouse xenograft tumor model. Therefore, the combination of Compound 6 with rituximab may clinically benefit patients with diffuse large B-cell lymphoma (DLBCL) .
- DLBCL diffuse large B-cell lymphoma
- Example 4 Effects of Compound 6 in combination with rituximab and bendamustine on mouse xenograft tumor model
- Bendamustine was an FDA approved drug for the treatment of B-cell non-Hodgkin's lymphoma.
- the anti-tumor effect of Compound 6 with bendamustine (B: 25 mg/kg, i.v. ) and rituximab (R: 10 mg/kg, i.v. ) in combination (BR) was subsequently evaluated in the same experiment.
- Compound 6 in combination with rituximab and bendamustine had no significant side effects (Figure 2B) and significantly increased the anti-tumor effect of each single agent in the OCI-LY8 human DLBCL cell mouse xenograft tumor model. Therefore, the combination of Compound 6 with rituximab and bendamustine may clinically benefit patients with diffuse large B-cell lymphoma (DLBCL) .
- DLBCL diffuse large B-cell lymphoma
- DOHH2 was a human follicular lymphoma (FL, belonging to NHL) cell line that was relatively sensitive to Compound 6 treatment. Therefore, this experiment established a model of FL mouse xenograft tumor derived from DOHH2 cells (Andrew J Souers et al., ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets. Nature Medicine vol 19, 202–208 (2013) ) , to evaluate the antitumor effect of Compound 6 in combination with BR.
- FL human follicular lymphoma
- the BR dual therapy showed effective anti-tumor activity with a T/C value of 1.4%(P ⁇ 0.01; 1/5 CR and 4/5 PR, the remission rate was 100%) .
- Compound 6 showed a significant anti-tumor effect after administration of 100 mg/kg, p.o., qd regimen, with a T/C value of 28% (P ⁇ 0.01) .
- the triple therapy of Compound 6 plus BR almost result in complete tumor regression with a T/C value of 0.2%(P ⁇ 0.001; 2/5 CR and 3/5 PR; the remission rate was 100%) .
- Compound 6 in combination with rituximab and bendamustine had no significant side effects (Figure 2B) and significantly increased the anti-tumor effect of each single drug in the human DOHH2 (FL) mouse xenograft tumor model. Therefore, the combination of Compound 6 with rituximab and bendamustine may clinically benefit patients with follicular lymphoma (FL) .
- Example 5 Effects of Compound 6 in combination with CHOP (i.e, cyclophosphamide, doxorubicin, vincristine, and prednisone) in DOHH2 (FL) model
- CHOP included: cyclophosphamide, 20 mg/kg, intraperitoneal injection, administered on the 1 st and 9 th days; doxorubicin, 2 mg/kg, intravenous injection, administered on the 1 st day; vincristine, 0.1 mg/kg, intravenous injection, administered on the 1 st and 9 th days; prednisone, 0.5 mg/kg, orally administered on the 1 st day.
- cyclophosphamide (batch number: 09121921) was purchased from Jiangsu Hengrui Medicine Co., Ltd. Cyclophosphamide was administered intraperitoneally. The injected dose was 10 mL/kg (0.2 mL/mouse) .
- Doxorubicin (batch number: 20061106) was purchased from Shanghai Richem Inc. Doxorubicin was administered by intravenous injection at a dose of 10 mL/kg (0.2 mL/mouse) . The agent was dissolved in saline.
- Vincristine (batch number: 0708v1) was purchased from Shenzhen Main Luck Pharmaceuticals Inc. Vincristine was administered by intravenous injection at a dose of 10 mL/kg (0.2 mL/mouse) . The agent was dissolved in saline.
- Prednisone (batch number: M0412A) was purchased from Dalian Meilun Biotechnology Co., Ltd.
- Prednisone was administered by oral gavage at a dose of 10 mL/kg (0.2 mL/mouse) .
- the agent was dissolved in 10%PEG 400 /5%EL /85%PBS.
- the dosage formulations were prepared freshly prior to use. The preparation and use of the dosage formulations were always carried out under sterile conditions.
- the T/C values of the group of single Compound 6 at 100 mg/kg dose and the group of CHOP treatment were 28% (P ⁇ 0.01) and 50% (P ⁇ 0.05) , respectively, without remission of PR or CR.
- Compound 6 in combination with CHOP showed significantly enhanced effect of growth inhibition with a T/C value of 9%(P ⁇ 0.001; 0/5 CR and 4/5 PR; remission rate 80%) .
Abstract
Description
Claims (25)
- A combination product comprising a Bcl-2 inhibitor and an anti-CD20 mAb.
- A combination product comprising a Bcl-2 inhibitor, an anti-CD20 mAb, and Bendamustine.
- A combination product comprising a Bcl-2 inhibitor and CHOP.
- The combination product according to any one of claims 1 to 3, wherein the Bcl-2 inhibitor is a compound of Formula I-Aor a pharmaceutically acceptable salt or solvate thereof:wherein:A isX 1, X 2 and X 3 are each independently selected from the group consisting of -CR 8= and -N=;R 1a and R 1b taken together with the carbon atom to which they are attached form a 3-, 4-, or 5-membered optionally substituted aliphatic ring; orR 1a and R 1b taken together with the carbon atom to which they are attached form a 4-or 5-membered optionally substituted heterocyclo;R 2 is selected from the group consisting of -NO 2, -SO 2CH 3, and -SO 2CF 3;R 2a is selected from the group consisting of hydrogen and X;R 3 is selected from the group consisting of hydrogen, -CN, -C≡CH, and -N (R 4a) (R 4b) ;R 4a is selected from the group consisting of optionally substituted C 1-6 alkyl, optionally substituted C 3-6 cycloalkyl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl;R 4b is selected from the group consisting of hydrogen and C 1-4 alkyl;R 5 is selected from the group consisting of optionally substituted C 1-6 alkyl, heterocyclo, cycloalkylalkyl, and heterocycloalkyl;R 6a, R 6c, R 6e, R 6f, and R 6g are each independently selected from the group consisting of hydrogen, optionally substituted C 1-6 alkyl, optionally substituted C 3-6 cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl;R 6b and R 6d are each independently selected from the group consisting of hydrogen, C 1-4 alkyl, and halogen;R 7 is selected from the group consisting of optionally substituted C 1-6 alkyl, heterocyclo, heteroalkyl, cycloalkylalkyl, and heterocycloalkyl; andR 8 is selected from the group consisting of hydrogen and halogen.
- The combination product according to any one of claims 1 to 2, wherein the anti-CD20 mAb is selected from the group consisting of: Rituximab, IF5, Ibritumomab tiuxetan, tositumomab, ocrelizumab, veltuzumab, ofatumumab, obinutuzumab, AME133V, Pro13192 and GA101, TRU-015.
- The combination product according to any one of claims 1-2 and 4-6, wherein the Bcl-2 inhibitor and the anti-CD20 mAb are administered simultaneously, sequentially or alternately.
- The combination product according to any one of claims 1-2 and 4-6, wherein the Bcl-2 inhibitor, anti-CD20 mAb and Bendamustine are administered simultaneously, sequentially or alternately.
- The combination product according to any one of claims 3 to 5, wherein the Bcl-2 inhibitor and CHOP are administered simultaneously, sequentially or alternately.
- The combination product according to any one of claims 1 to 9, which further comprises a pharmaceutically acceptable carrier, diluent or excipient.
- Use of a Bcl-2 inhibitor and an anti-CD20 mAb in the manufacture of a medicament for the prevention and/or treatment of a disease selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- Use of a Bcl-2 inhibitor, an anti-CD20 mAb, and Bendamustine in the manufacture of a medicament for the prevention and/or treatment of a disease selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- Use of a Bcl-2 inhibitor and CHOP in the manufacture of a medicament for the prevention and/or treatment of a disease, wherein the disease is cancer.
- A combination product for the prevention and/or treatment of a disease, wherein the combination product comprises a Bcl-2 inhibitor and an anti-CD20 mAb, and the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- A combination product for the prevention and/or treatment of a disease, wherein the combination product comprises a Bcl-2 inhibitor, an anti-CD20 mAb and Bendamustine, and the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- A combination product for the prevention and/or treatment of a disease, wherein the combination comprises a Bcl-2 inhibitor and CHOP, and the disease is cancer.
- A method for the prevention and/or treatment of a disease, comprising administering to a subject in need thereof a prophylactically and/or therapeutically effective amount of a Bcl-2 inhibitor and an anti-CD20 mAb, wherein the disease is selected from the group consisting of cancer, Rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- The method according to claim 17, wherein the cancer is selected from the group consisting of: bladder cancer, breast cancer, cervical cancer, colon cancer (including colorectal cancer) , esophageal cancer, head and neck cancer, liver cancer, lung cancer (small cell and non-small cell) , melanoma, myeloma, neuroblastoma, ovarian cancer, pancreatic cancer, prostate cancer, kidney cancer, sarcoma (including osteosarcoma) , skin cancer (including squamous cell cancer) , gastric cancer, testicular cancer, thyroid cancer, uterine cancer, mesothelioma, cholangiocarcinoma, leiomyosarcoma, liposarcoma, melanoma, nasopharyngeal carcinoma, neuroendocrine carcinoma, ovarian cancer, renal cancer, salivary gland cancer, or metastases induced by spindle cancer, non-Hodgkin’s lymphoma (NHL) , Hodgkin's lymphoma, acute myeloid leukemia (AML) , acute lymphoblastic leukemia (ALL) , diffuse large B-cell lymphoma (DLBCL) , follicular lymphoma (FL) , chronic lymphocytic leukemia (CLL) /small lymphocytic lymphoma (SLL) , marginal zone lymphoma (MZL) , chronic myelogenous leukemia (CML) , mantle cell lymphoma (MCL) , Waldenstrom's macroglobulinemia (WM) .
- The method according to claim 17 or 18, wherein the Bcl-2 inhibitor or a pharmaceutically acceptable salt or solvate thereof is administered in an amount of about 0.0025 -1500 mg/day, and the anti-CD20 mAb is administered in an amount of about 0.0025 -800 mg/day.
- A method for the prevention and/or treatment of a disease, comprising administering to a subject in need thereof a prophylactically and/or therapeutically effective amount of a Bcl-2 inhibitor, an anti-CD20 mAb and Bendamustine, wherein the disease is selected from the group consisting of cancer, rheumatoid arthritis (RA) , granulomatosis with polyangiitis (GPA) and microscopic polyangiitis.
- The method according to claim 20, wherein the cancer is selected from the group consisting of: bladder cancer, breast cancer, cervical cancer, colon cancer (including colorectal cancer) , esophageal cancer, head and neck cancer, liver cancer, lung cancer (small cell and non-small cell) , melanoma, myeloma, neuroblastoma, ovarian cancer, pancreatic cancer, prostate cancer, kidney cancer, sarcoma (including osteosarcoma) , skin cancer (including squamous cell cancer) , gastric cancer, testicular cancer, thyroid cancer, uterine cancer, mesothelioma, cholangiocarcinoma, leiomyosarcoma, liposarcoma, melanoma, nasopharyngeal carcinoma, neuroendocrine carcinoma, ovarian cancer, renal cancer, salivary gland cancer, or metastases induced by spindle cancer, non-Hodgkin’s lymphoma (NHL) , Hodgkin's lymphoma, acute myeloid leukemia (AML) , acute lymphoblastic leukemia (ALL) , diffuse large B-cell lymphoma (DLBCL) , follicular lymphoma (FL) , chronic lymphocytic leukemia (CLL) /small lymphocytic lymphoma (SLL) , marginal zone lymphoma (MZL) , chronic myelogenous leukemia (CML) , mantle cell lymphoma (MCL) , Waldenstrom's macroglobulinemia (WM) .
- The method according to claim 20 or 21, wherein the Bcl-2 inhibitor or a pharmaceutically acceptable salt or solvate thereof is administered in an amount of about 0.0025 -1500 mg/day, the anti-CD20 mAb is administered in an amount of about 0.0025 -800 mg/day, and the Bendamustine is administered in an amount of about 0.0025 -500 mg/day.
- A method for the prevention and/or treatment of a disease comprising administering to a subject in need thereof a prophylactically and/or therapeutically effective amount of a Bcl-2 inhibitor and CHOP, wherein the disease is cancer.
- The method according to claim 23, wherein the cancer is selected from the group consisting of: bladder cancer, breast cancer, cervical cancer, colon cancer (including colorectal cancer) , esophageal cancer, head and neck cancer, liver cancer, lung cancer (small cell and non-small cell) , melanoma, myeloma, neuroblastoma, ovarian cancer, pancreatic cancer, prostate cancer, kidney cancer, sarcoma (including osteosarcoma) , skin cancer (including squamous cell cancer) , gastric cancer, testicular cancer, thyroid cancer, uterine cancer, mesothelioma, cholangiocarcinoma, leiomyosarcoma, liposarcoma, melanoma, nasopharyngeal carcinoma, neuroendocrine carcinoma, ovarian cancer, renal cancer, salivary gland cancer, or metastases induced by spindle cancer, non-Hodgkin’s lymphoma (NHL) , Hodgkin's lymphoma, acute myeloid leukemia (AML) , acute lymphoblastic leukemia (ALL) , diffuse large B-cell lymphoma (DLBCL) , follicular lymphoma (FL) , chronic lymphocytic leukemia (CLL) /small lymphocytic lymphoma (SLL) , marginal zone lymphoma (MZL) , chronic myelogenous leukemia (CML) , mantle cell lymphoma (MCL) , Waldenstrom's macroglobulinemia (WM) .
- The method according to claim 23 or 24, wherein the Bcl-2 inhibitor or a pharmaceutically acceptable salt or solvate thereof is administered in an amount of about 0.0025 -1500 mg/day, and the CHOP is administered in an amount of about 0.0025-500 mg/day.
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
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EA202091963A EA202091963A1 (en) | 2018-07-31 | 2019-07-22 | SYNERGIC ANTITUMOR EFFECT OF Bcl-2 INHIBITOR IN COMBINATION WITH RITUXIMAB AND / OR BENDAMUSTIN OR Bcl-2 INHIBITOR IN COMBINATION WITH CHOP |
UAA202005954A UA125241C2 (en) | 2018-07-31 | 2019-07-22 | Synergistic antitumor effect of bcl-2 inhibitor combined with rituximab and/orbendamustine or bcl-2 inhibitor combined with chop |
EP19845466.2A EP3672591B1 (en) | 2018-07-31 | 2019-07-22 | Synergistic antitumor effect of bcl-2 inhibitor combined with rituximab and/or bendamustine or bcl-2 inhibitor combined with chop |
CA3092753A CA3092753C (en) | 2018-07-31 | 2019-07-22 | Synergistic antitumor effect of bcl-2 inhibitor combined with rituximab |
BR112020019134-5A BR112020019134A2 (en) | 2018-07-31 | 2019-07-22 | combination products comprising bcl-2 inhibitor and anti-cd20 mab, or bcl-2 inhibitor, anti-cd20 mab and bendamustine, or bcl-2 and chop inhibitor and therapeutic uses thereof |
AU2019315466A AU2019315466B2 (en) | 2018-07-31 | 2019-07-22 | Synergistic antitumor effect of Bcl-2 inhibitor combined with rituximab and/or bendamustine or Bcl-2 inhibitor combined with CHOP |
KR1020207026501A KR20200139139A (en) | 2018-07-31 | 2019-07-22 | Synergistic anti-tumor effects of Bcl-2 inhibitors in combination with rituximab and/or bendamustine or Bcl-2 inhibitors in combination with CHOP |
MX2020009759A MX2020009759A (en) | 2018-07-31 | 2019-07-22 | Synergistic antitumor effect of bcl-2 inhibitor combined with rituximab and/or bendamustine or bcl-2 inhibitor combined with chop. |
US16/648,593 US11554127B2 (en) | 2018-07-31 | 2019-07-22 | Synergistic antitumor effect of Bcl-2 inhibitor combined with rituximab and/or bendamustine or Bcl-2 inhibitor combined with CHOP |
JP2020570625A JP2021516262A (en) | 2018-07-31 | 2019-07-22 | Synergistic antitumor effect of Bcl-2 inhibitor combined with rituximab and / or bendamustine or Bcl-2 inhibitor combined with CHOP |
IL277309A IL277309A (en) | 2018-07-31 | 2020-09-13 | Synergistic antitumor effect of bcl-2 inhibitor combined with rituximab and/or bendamustine or bcl-2 inhibitor combined with chop |
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EA202091963A1 (en) | 2021-05-13 |
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US20210361678A1 (en) | 2021-11-25 |
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IL277309A (en) | 2020-10-29 |
CN110772640B (en) | 2023-02-03 |
EP3672591A4 (en) | 2021-01-13 |
EP3672591A1 (en) | 2020-07-01 |
CA3092753C (en) | 2023-10-17 |
CN110772640A (en) | 2020-02-11 |
GEP20237460B (en) | 2023-01-25 |
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